US5280123A - Organophosphorus compounds and its insecticides acaricides and nematocides containing same - Google Patents
Organophosphorus compounds and its insecticides acaricides and nematocides containing same Download PDFInfo
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- US5280123A US5280123A US07/726,211 US72621191A US5280123A US 5280123 A US5280123 A US 5280123A US 72621191 A US72621191 A US 72621191A US 5280123 A US5280123 A US 5280123A
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-nitrogen bonds
- A01N57/32—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-nitrogen bonds containing heterocyclic radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6503—Five-membered rings
- C07F9/6506—Five-membered rings having the nitrogen atoms in positions 1 and 3
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/572—Five-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/576—Six-membered rings
- C07F9/59—Hydrogenated pyridine rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6509—Six-membered rings
- C07F9/6512—Six-membered rings having the nitrogen atoms in positions 1 and 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having three nitrogen atoms as the only ring hetero atoms
- C07F9/6521—Six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6527—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and oxygen atoms as the only ring hetero atoms
- C07F9/653—Five-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6536—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and sulfur atoms with or without oxygen atoms, as the only ring hetero atoms
- C07F9/6539—Five-membered rings
Definitions
- the present invention relates to an organophosphorus compound represented by the following general formula (I): ##STR3## [wherein R 1 and R 2 each represents a C 1 to C 4 alkyl group; X represents O, S, CH 2 , CH--R 3 (wherein R 3 represents a C 1 to C 3 alkyl group), NH or N--R 4 ⁇ wherein R 4 represents a C 1 to C 4 alkyl group (the alkyl group may be substituted with at least one group selected from the group consisting of alkoxy, alkylthio, cyano, alkoxyalkyloxy and alkylamino groups and halogen atoms), an alkenyl group which may be substituted with halogen atoms, an alkynyl group which may be substituted with halogen atoms, a phosphoric acid ester radical, a cyano group, a group of the following general formula (II): ##STR4## (wherein R 5 represents an alkyl or alky
- the compound of formula (I) according to the present invention specifically excludes an organophosphorus compound of the general formula (I) in which R 1 and R 2 are C 1 to C 4 alkyl groups respectively, X is NH, Z is a cyanoimino group or a nitroimino group and A is an ethylene group which may be substituted with C 1 to C 3 alkyl groups or a trimethylene group which may be substituted with C 1 to C 3 alkyl groups.
- the present invention also relates to a method for preparing the compound, of formula (I), and insecticides, acaricides and nematocides which comprise the compound as an active ingredient.
- organophosphorus compounds having an imidazolidinyl group have been investigated and developed.
- Japanese Unexamined Patent Publication No. Sho 61-267594 and Japanese Unexamined Patent Publication No. Hei 2-793 disclose that these compounds can be used as insecticides, acaricides, nematocides and agents for killing soil insect pests.
- these patents simply disclose organophosphorus compounds having an imidazolidine skeleton which carries an oxygen or sulfur atom on the 2-position.
- the insecticidal, acaricidal and nematocidal effects of these compounds are insufficient and are not necessarily satisfactory.
- an object of the present invention is to provide a novel organophosphorus compound represented by the foregoing general formula (I).
- Another object of the present invention is to provide a method for preparing a novel organophosphorus compound represented by the foregoing general formula (I).
- a further object of the present invention is to provide an agricultural chemical having insecticidal, acaricidal and nematocidal effects higher than those attained by conventional agricultural chemicals and exhibiting very low toxicity to warm-blooded animals.
- the inventors of this invention have synthesized a variety of organophosphorus compounds carrying an imidazolidinyl group and have investigated the insecticidal, acaricidal and nematocidal activities of the organophosphorus compounds having an imidazolidine skeleton which carries a specific substituent on the 2-position in order to develop effective insecticides, acaricides and nematocides.
- the compound of the present invention represented by the following general formula (I): ##STR5##
- R 1 and R 2 each represents a C 1 to C 4 alkyl group
- X represents O, S, CH 2 , CH--R 3 (wherein R 3 represents a C 1 to C 3 alkyl group)
- NH or N--R 4 ⁇ wherein R 4 represents a C 1 to C 4 alkyl group (the alkyl group may be substituted with at least one group selected from the group consisting of alkoxy, alkylthio, cyano, alkoxyalkyloxy and alkylamino groups and halogen atoms), an alkenyl group which may be substituted with halogen atoms, an alkynyl group which may be substituted with halogen atoms, a phosphoric acid ester radical, a cyano group
- the compound of formula (I) according to the present invention specifically excludes an organophosphorus compound of the general formula (I) in which R 1 and R 2 are C 1 to C 4 alkyl groups respectively, X is NH, Z is a cyanoimino group or a nitroimino group and A is an ethylene group which may be substituted with C 1 to C 3 alkyl groups or a trimethylene group which may be substituted with C 1 to C 3 alkyl groups.
- organophosphorus compounds do not give off any bad or irritating odor and have low toxicity to warm-blooded animals. Therefore, they can widely be used and thus have very high usefulness.
- organophosphorus compounds represented by the foregoing general formula (I) also include stereoisomers such as optical isomers.
- the organophosphorus compounds when X is the group NH, the organophosphorus compounds may exist in the form of a tautomer represented by the following general formula (I'): ##STR7## (wherein R 1 , R 2 , Z and A are the same as those defined above). These compounds (tautomeric isomers) are likewise included in the scope of the compound of the present invention.
- the compounds of the present invention can be prepared in accordance with, for instance, any one of the following three methods. ##STR8## (Wherein R 1 , R 2 , R 4 , X, Z and A are the same as those defined above and Hal means a halogen atom).
- the foregoing reactions are in general carried out at a temperature ranging from -100° to +60° C. and preferably from -80° to +30° C. Moreover, these reactions are performed in the presence of a deacidifying agent, examples of which include organic lithium compounds such as n-butyl lithium, t-butyl lithium and phenyl lithium; inorganic bases such as sodium hydride, potassium hydride, metallic sodium, sodium hydroxide and potassium hydroxide; alkoxides such as sodium methoxide, sodium ethoxide and potassium t-butoxide; and organic bases such as triethylamine and pyridine.
- a deacidifying agent examples of which include organic lithium compounds such as n-butyl lithium, t-butyl lithium and phenyl lithium; inorganic bases such as sodium hydride, potassium hydride, metallic sodium, sodium hydroxide and potassium hydroxide; alkoxides such as sodium methoxide, sodium ethoxide and potassium
- these reactions are desirably carried out in the presence of a solvent.
- solvents include aromatic hydrocarbons such as benzene, toluene, xylene and chlorobenzene; cyclic or non-cyclic aliphatic hydrocarbons such as hexane and cyclohexane; ethers such as diethyl ether, methyl ethyl ether, dioxane and tetrahydrofuran; nitriles such as acetonitrile, propionitrile and acrylonitrile; and aprotic polar solvents such as dimethylformamide, dimethylsulfoxide, sulfolane and hexamethyl-phosphoric acid triamide.
- the compounds of the present invention exhibit excellent activity as active ingredients of insecticides, acaricides and nematocides.
- the compounds of the present invention are effective for controlling, for instance, agricultural and horticultural pests such as Coleoptera (for instance, Scarabaeidae, Chrysomelidae, Henosepilachna vigintioctopunctate and Lissorhoptrus oryzophilus), Lepidoptera (for instance, Mamestra brassicae, Pieris rapae, Plutera xylostella, Noctuidae, Adoxophyes orana and Chilo suppressalis), Hemiptera (for instance, Delphacidae, Deltocephalidae, Aleyrodidae, Aphididae and Scales) and Thysanoptera (for instance, Scirtothrips dorsalis and Thrips pulmi); Sanitary pests such as Mosquitoes, Flies
- soil insect pest means, for instance, Gastropoda such as slugs and snails; Isopoda such as Armadillidium vulgare and Sow bugs.
- insect pest such as Dicofol, organophosphorus compound-resistant plant parasitic mites, organophosphorus compound-resistant Aphididae and Musca domestica.
- the compounds of the present invention are used as active ingredients of insecticidal, acaricidal, nematocidal compositions and composition for killing or controlling soil pest insect, they may be used as such, but may in general be formed into a variety of formulations together with adjuvants such as emulsifiable concentrates, dusts, wettable powders, liquid formulations, aerosols and pastes like conventional formulations of agricultural chemicals.
- the formulations in general comprise 0.5 to 90 parts by weight of the active ingredient and 10 to 99.5 parts by weight of an adjuvant. When these formulations are practically used, they can be applied as such or after diluting them with a diluent such as water to a desired concentration.
- adjuvant herein means carriers, emulsifying agents, suspending agents, dispersing agents, spreaders, penetrants, wetting agents, thickeners and stabilizers. These adjuvants may, if necessary, be added in an appropriate amount.
- the carriers can roughly be classified into solid carriers and liquid carriers. Examples of the solid carriers include vegetable and animal powder such as starches, active carbon, soybean flour, wheat flour, wood powder, fish meal and powdered milk; and mineral powders such as talc, kaolin, bentonite, calcium carbonate, zeolite, diatomaceous earth, white carbon, clay, alumina and powdered sulfur.
- liquid carriers examples include water; alcohols such as methyl alcohol and ethylene glycol; ketones such as acetone and methyl ethyl ketone; ethers such as dioxane and tetrahydrofuran; aliphatic hydrocarbons such as kerosine; aromatic hydrocarbons such as xylene, trimethylbenzene, tetramethylbenzene, cyclohexane and solvent naphtha; halogenated hydrocarbons such as chloroform and chlorobenzene; amides such as dimethylformamide; esters such as ethyl acetate and glycerin esters of fatty acids; nitriles such as acetonitrile; and sulfur atom-containing compounds such as dimethylsulfoxide.
- alcohols such as methyl alcohol and ethylene glycol
- ketones such as acetone and methyl ethyl ketone
- ethers such as dioxane and tetrahydrofuran
- the compounds of the present invention may be admixed with or used simultaneously with other agricultural chemicals such as insecticides, acaricides, nematocides, bactericides, antiviral agents, attractants, herbicides and plant growth regulators. In admixtures, greater effectiveness may sometimes be attained.
- insecticides, acaricides or nematocides include organophosphorus acid ester compounds such as DDVP, Diazinon, Malathion, Fenitrothion, Prothiofos, Dioxabenzofos and Acephate; carbamate compounds such as Carbaryl, Propoxur, Oxamyl, Carbofuran and Methomyl; organochlorine compounds such as Dicofol and Tetradifon; organometal compounds such as Cyhexatin and Fenbutatin oxide; pyrethroid compounds such as Fenvalerate, Permethrin, Deltamethrin and Bifenthrin; urea compounds such as Diflubenzuron, Teflubenzuron and Chlorfluazuron; heterocyclic compounds such as Buprofezin and Hexythiazox; and other compounds such as dinitro compounds, organosulfur compounds, amidine compounds and triazine compounds.
- organophosphorus acid ester compounds such as DDVP
- bactericides are organophosphorus compounds such as Iprobenfos, Edifenphos and Phosethyl-aluminum; organocopper compounds such as oxyguinoline copper, copper terephthalate; organochlorine compounds such as Fthalide and Chlorothalonil; dithiocarbamate compounds such as Maneb, Zineb and Propineb; dicarboximide compounds such as Iprodione, Vinclozolin and Procymidone; azole compounds such as Triadimefon, Bitertanol, Etaconazole, Propiconazole and Penconazole; benzimidazole compounds such as Thiophanate-methyl and Benomyl; carbinol compounds such as Fenarimol and Flutriafol; benzanilide compounds such as Mepronil and Flutolanil; phenylamide compounds such as Metalaxyl and Oxadixyl; and other compounds such as piperazine compounds, quinoxaline
- the insecticides, acaricides and nematocides which comprise, as active ingredient, the compounds of the present invention are effective for controlling a variety of deleterious insects, harmful mites, destructive nematodes and harmful soil insect pests.
- These agricultural chemicals or formulations are applied at a concentration ranging from 1 to 20,000 ppm, desirably 20 to 2,000 ppm expressed in terms of the amount of the active ingredient.
- concentration of these active ingredients can be appropriately adjusted depending on various factors such as shapes of the formulations, methods, purposes, time and places of application as well as the condition of infestation of insect pest.
- the insect pest when aquatic insect pests are to be controlled, the insect pest can be controlled by spraying a solution of the compound having a concentration falling within the range defined above and, therefore, the concentration of the active ingredient required for controlling the aquatic insect pest is lower than that defined above.
- the amount of the agricultural chemicals or formulations to be applied per unit area (per 10 a) ranges from about 0.1 to 5,000 g and preferably 10 to 1,000 g expressed in terms of the amount of the active ingredient, but in a particular case, they may be applied in an amount outside the range defined above.
- formulations or dilute solutions thereof which comprise the compounds of the present invention can be performed according to any manner of application usually adopted, for instance, spraying (such as spraying, dusting, misting, atomizing, granule application and application on water surface); soil applications (such as mixing and drench); surface applications (such as coating, dressing and painting); and poison bait. It is also possible to control the development and growth of harmful insect pests, in particular deletrious insects through the action of excreta obtained by admixing the foregoing active ingredient to feed and giving the feed to domestic animals. Further, they can also be applied in accordance with ultra low volume application. In this method, the chemicals or formulations can comprise 100% active ingredient.
- the dichloromethane phase was washed with water, dried over anhydrous magnesium sulfate, the dichloromethane was distilled off under reduced pressure and the residue obtained was purified by silica gel column chromatography (eluent: ethyl acetate) to give 0.50 g of Compound No. 2 as an oily substance.
- reaction solution was poured into ice water and then extracted with ethyl acetate.
- the ethyl acetate phase was washed with water, dried over anhydrous magnesium sulfate, the ethyl acetate was distilled off under reduced pressure and the residue obtained was purified by silica gel column chromatography (eluent: chloroform) to thus give 1.10 g of Compound No. 29 as an oily substance.
- the emulsifiable concentrate obtained by Formulation Example 2 was diluted with water to 500 ppm and 50 ppm and the resulting diluted emulsions were sprayed on leaves of chinese cabbage. After air-drying, the leaves were introduced into a plastic container having a size of 21 cm (height) ⁇ 13 cm (width) ⁇ 3 cm (depth), then 10 third instar larvae of common cutworm were put on the leaves. The container was then placed in a thermostated room maintained at 26° C. After 2 days, the number of surviving larvae was recorded to obtain the mortality (%) (repeated two times). The results thus obtained are summarized in the following Table 3.
- the Comparative Compound A as set forth in Table 3 is a compound represented by the following structural formula and disclosed in Japanese Unexamined Patent Publication No. Sho 61-267594: ##STR22##
- the emulsifiable concentrate obtained by Formulation Example 2 was diluted with water to 500 ppm and the seedlings of rice plant were immersed therein for 10 seconds. After air-drying, the seedlings whose roots were wrapped round with absorbent cotton were introduced into a test tube, then 10 second instar larvae of green rice leafhopper were put into the test tube, the opening thereof was closed with gauze. The tube was placed in a thermostated room maintained at 26° C. After 2 days, the number of surviving larvae was recorded to obtain the mortality (%) (repeated two times). The results thus obtained are summarized in the following Table 4.
- the comparative Compound A as set forth in Table 4 is the same as that defined above in connection with Table 3.
- a kidney bean leaf was cut into 3 ⁇ 5 cm 2 .
- the leaf was put on a filter paper wetted with water for preventing drying of the leaf and 20 female adults of kanzawa spider mite were released on the leaf.
- 500 ppm and 50 ppm of concentration of active ingredient prepared by diluting with water the emulsifiable concentrate obtained by Formulation Example 2 were sprayed on the leaf.
- the mites were held in a thermostated room maintained at 26° C. After 24 hours, the number of surviving adults were recorded to obtain the mortality (%) (repeated two times).
- the results thus obtained are summarized in the following Table 5.
- the Comparative Compound A is the same as that defined above in connection with Table 3.
- the root-knot index was evaluated on the basis of the following evaluation criteria:
- Comparative Compound B is a compound (oxamyl) represented by the following structural formula: ##STR23##
- the compounds of the present invention represented by the foregoing general formula (I) exhibit effectiveness in controlling harmful insects, mites and nematodes and thus can be used as novel insecticides, acaricides and nematocides which do not give off a bad or irritating odor and have low toxicity to warm-blooded animals.
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Abstract
Insecticidal, acaricidal or nematocidal compositions which comprise organophosphorus compounds of the formula (* CHEMICAL STRUCTURE *) wherein R1 and R2 each represents a C1 to C4 alkyl group; X represents NH or N-R4 wherein R4 represents an alkyl; an alkenyl; an alkynyl; a phosphoric acid ester radical; a cyano group; a group of formula (II): (* CHEMICAL STRUCTURE *) (II) (wherein R5 represents an alkyl or alkylamino group); or a group of the formula: -(R6)n-CO-R7 (wherein n is 0 or 1; R6 represents a methylene or an ethylene group; and R7 represents an alkyl, an alkoxy, an alkylthio group, an alkylamino group or a hydrogen atom); Z represents N-R8 (wherein R8 represents a nitro group, a cyano group, an alkylsulfonyl group, a tosyl group or an alkylcarbonyl group) or a group represented by the formula: C(CN)R9 (wherein R9 represents a cyano group or an alkoxycarbonyl group); and A represents an ethylene group which may be substituted with C1 to C3 alkyl, excluding organophosphorus compounds of formula (I) in which R1 and R2 are C1 to C4 alkyl groups, X is NH, Z is a cyanoimino group or a nitroimino group and A is an ethylene group.
Description
1. Field of the Invention
The present invention relates to an organophosphorus compound represented by the following general formula (I): ##STR3## [wherein R1 and R2 each represents a C1 to C4 alkyl group; X represents O, S, CH2, CH--R3 (wherein R3 represents a C1 to C3 alkyl group), NH or N--R4 {wherein R4 represents a C1 to C4 alkyl group (the alkyl group may be substituted with at least one group selected from the group consisting of alkoxy, alkylthio, cyano, alkoxyalkyloxy and alkylamino groups and halogen atoms), an alkenyl group which may be substituted with halogen atoms, an alkynyl group which may be substituted with halogen atoms, a phosphoric acid ester radical, a cyano group, a group of the following general formula (II): ##STR4## (wherein R5 represents an alkyl or alkylamino group which may be substituted with halogen atoms) or a group represented by the following general formula: --(R6)n --CO--R7 (wherein n is 0 or 1; R6 represents a methylene group which may be substituted with alkyl groups, or an ethylene group which may be substituted with alkyl groups; R7 represents an alkyl group which may be substituted with halogen atoms, an alkoxy group which may be substituted with halogen atoms, an alkylthio group, an alkylamino group or a hydrogen atom)}; Z represents a group represented by the general formula: N--R8 (R8 represents a nitro group, a cyano group, an alkylsulfonyl group which may be substituted with halogen atoms, a tosyl group or an alkylcarbonyl group which may be substituted with halogen atoms) or a group represented by the general formula: C(CN)R9 (wherein R9 represents a cyano group or an alkoxycarbonyl group); and A represents an ethylene group which may be substituted with C1 to C3 alkyl groups, a trimethylene group which may be substituted with C1 to C3 alkyl groups or a group represented by the general formula: --CH2 NR10 CH2 -- (wherein R10 is a C1 to C3 alkyl group)]. The compound of formula (I) according to the present invention specifically excludes an organophosphorus compound of the general formula (I) in which R1 and R2 are C1 to C4 alkyl groups respectively, X is NH, Z is a cyanoimino group or a nitroimino group and A is an ethylene group which may be substituted with C1 to C3 alkyl groups or a trimethylene group which may be substituted with C1 to C3 alkyl groups. The present invention also relates to a method for preparing the compound, of formula (I), and insecticides, acaricides and nematocides which comprise the compound as an active ingredient.
2. Prior Art Statement
Recently, organophosphorus compounds having an imidazolidinyl group have been investigated and developed. For instance, Japanese Unexamined Patent Publication No. Sho 61-267594 and Japanese Unexamined Patent Publication No. Hei 2-793 disclose that these compounds can be used as insecticides, acaricides, nematocides and agents for killing soil insect pests. However, these patents simply disclose organophosphorus compounds having an imidazolidine skeleton which carries an oxygen or sulfur atom on the 2-position. Moreover, the insecticidal, acaricidal and nematocidal effects of these compounds are insufficient and are not necessarily satisfactory.
Accordingly, an object of the present invention is to provide a novel organophosphorus compound represented by the foregoing general formula (I).
Another object of the present invention is to provide a method for preparing a novel organophosphorus compound represented by the foregoing general formula (I).
A further object of the present invention is to provide an agricultural chemical having insecticidal, acaricidal and nematocidal effects higher than those attained by conventional agricultural chemicals and exhibiting very low toxicity to warm-blooded animals.
The inventors of this invention have synthesized a variety of organophosphorus compounds carrying an imidazolidinyl group and have investigated the insecticidal, acaricidal and nematocidal activities of the organophosphorus compounds having an imidazolidine skeleton which carries a specific substituent on the 2-position in order to develop effective insecticides, acaricides and nematocides. As a result, the inventors have found out that excellent control of harmful insect pests can be achieved by an organophosphorus compound (hereinafter referred to as "the compound of the present invention") represented by the following general formula (I): ##STR5## [wherein R1 and R2 each represents a C1 to C4 alkyl group; X represents O, S, CH2, CH--R3 (wherein R3 represents a C1 to C3 alkyl group), NH or N--R4 {wherein R4 represents a C1 to C4 alkyl group (the alkyl group may be substituted with at least one group selected from the group consisting of alkoxy, alkylthio, cyano, alkoxyalkyloxy and alkylamino groups and halogen atoms), an alkenyl group which may be substituted with halogen atoms, an alkynyl group which may be substituted with halogen atoms, a phosphoric acid ester radical, a cyano group, a group of the following general formula (II): ##STR6## (wherein R5 represents an alkyl or alkylamino group which may be substituted with halogen atoms) or a group represented by the following general formula: --(R6)n --CO--R7 (wherein n is 0 or 1; R6 represents a methylene group which may be substituted with alkyl groups, or an ethylene group which may be substituted with alkyl groups; R7 represents an alkyl group which may be substituted with halogen atoms, an alkoxy group which may be substituted with halogen atoms, an alkylthio group, an alkylamino group or a hydrogen atom)}; Z represents a group represented by the general formula: N--R8 (R8 represents a nitro group, a cyano group, an alkylsulfonyl group which may be substituted with halogen atoms, a tosyl group or an alkylcarbonyl group which may be substituted with halogen atoms) or a group represented by the general formula: C(CN)R9 (wherein R9 represents a cyano group or an alkoxycarbonyl group); and A represents an ethylene group which may be substituted with C1 to C3 alkyl groups, a trimethylene group which may be substituted with C1 to C3 alkyl groups or a group represented by the general formula: --CH2 NR10 CH2 -- (wherein R10 is a C1 to C3 alkyl group)]. The compound of formula (I) according to the present invention specifically excludes an organophosphorus compound of the general formula (I) in which R1 and R2 are C1 to C4 alkyl groups respectively, X is NH, Z is a cyanoimino group or a nitroimino group and A is an ethylene group which may be substituted with C1 to C3 alkyl groups or a trimethylene group which may be substituted with C1 to C3 alkyl groups. Thus, the present invention has completed on the basis of the foregoing finding.
These organophosphorus compounds do not give off any bad or irritating odor and have low toxicity to warm-blooded animals. Therefore, they can widely be used and thus have very high usefulness.
The organophosphorus compounds represented by the foregoing general formula (I) also include stereoisomers such as optical isomers. In addition, in the general formula (I), when X is the group NH, the organophosphorus compounds may exist in the form of a tautomer represented by the following general formula (I'): ##STR7## (wherein R1, R2, Z and A are the same as those defined above). These compounds (tautomeric isomers) are likewise included in the scope of the compound of the present invention.
The compounds of the present invention can be prepared in accordance with, for instance, any one of the following three methods. ##STR8## (Wherein R1, R2, R4, X, Z and A are the same as those defined above and Hal means a halogen atom).
The foregoing reactions are in general carried out at a temperature ranging from -100° to +60° C. and preferably from -80° to +30° C. Moreover, these reactions are performed in the presence of a deacidifying agent, examples of which include organic lithium compounds such as n-butyl lithium, t-butyl lithium and phenyl lithium; inorganic bases such as sodium hydride, potassium hydride, metallic sodium, sodium hydroxide and potassium hydroxide; alkoxides such as sodium methoxide, sodium ethoxide and potassium t-butoxide; and organic bases such as triethylamine and pyridine.
In addition, these reactions are desirably carried out in the presence of a solvent. Examples of such solvents include aromatic hydrocarbons such as benzene, toluene, xylene and chlorobenzene; cyclic or non-cyclic aliphatic hydrocarbons such as hexane and cyclohexane; ethers such as diethyl ether, methyl ethyl ether, dioxane and tetrahydrofuran; nitriles such as acetonitrile, propionitrile and acrylonitrile; and aprotic polar solvents such as dimethylformamide, dimethylsulfoxide, sulfolane and hexamethyl-phosphoric acid triamide.
Typical examples of the compounds of the present invention will now be listed in the following Table 1. Each compound will hereinafter be described by the corresponding number of the compound. ##STR9##
In the following Table 1, the symbol "←" as set forth in the column "←A-" represents a bond with X and "ph" means a p-phenylene group.
TABLE 1-1
__________________________________________________________________________
Comp. No.
R.sup.1
R.sup.2
←A--
X Z Physical Property
__________________________________________________________________________
1 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
--(CH.sub.2).sub.2 --
N--CH.sub.3
N--NO.sub.2
m.p.: 46.0˜48.0° C.
2 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
--(CH.sub.2).sub.2 --
N--C.sub.2 H.sub.5
N--NO.sub.2
oily substance
3 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
--(CH.sub.2).sub.2 --
N--CH.sub.3
N-CN oily substance
4 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
--(CH.sub.2).sub.2 --
N--C.sub.2 H.sub.5
N-CN oily substance
5 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
--(CH.sub.2).sub.2 --
N-n-C.sub.3 H.sub.7
N-CN oily substance
6 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
--(CH.sub.2).sub.2 --
N-n-C.sub.4 H.sub.9
N-CN oily substance
7 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
--(CH.sub.2).sub.2 --
NH C(CN).sub.2
oily substance
8 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
--(CH.sub.2).sub.2 --
NH N--SO.sub.2 -ph-4-CH.sub.3
oily substance
9 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
--(CH.sub.2).sub.2 --
NH N--SO.sub.2 CH.sub.3
oily substance
__________________________________________________________________________
TABLE 1-2
__________________________________________________________________________
Comp. Physical
No. R.sup.1
R.sup.2
←A
X Z Property
__________________________________________________________________________
10 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
S NSO.sub.2 CH.sub.3
oily substance
11 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
S NCN oily substance
12 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
S NNO.sub.2
oily substance
13 C.sub.2 H.sub.5
sec-C.sub.4 H.sub.9
(CH.sub.2).sub.3
NCH.sub.3 NCN oily substance
14 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
##STR10## NCN oily substance
15 C.sub.2 H.sub.5
sec-C.sub.4 H.sub.9
(CH.sub.2).sub.2
NCH(CH.sub.3).sub.2
NCN oily substance
16 C.sub.2 H.sub.5
sec-C.sub.4 H.sub.9
(CH.sub.2).sub. 2
NCH.sub.3 NCN m.p.: 45.0˜47.0° C.
17 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.3
NCH.sub.3 C(CN).sub.2
oily substance
18 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NCH.sub.3 C(CN).sub.2
oily substance
19 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NCH.sub.3 NSO.sub.2 CH.sub.3
oily substance
__________________________________________________________________________
TABLE 1-3
__________________________________________________________________________
Comp. Physical
No. R.sup.1
R.sup.2
←A X Z Property
__________________________________________________________________________
20 C.sub.2 H.sub.5
sec-C.sub.4 H.sub.9
##STR11##
NCH.sub.3 C(CN).sub.2
m.p.: 73.0˜76.0° C.
21 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
CH.sub.2 NCH.sub.2
NH NNO.sub.2
oily substance
22 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
CH.sub.2 NCH.sub.2
NCH.sub.3 NNO.sub.2
oily substance
23 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
CH.sub.2 NCH.sub.2
N-n-CH.sub.3 H.sub.7
NNO.sub.2
oily substance
24 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NCH.sub.2 CHCH.sub.2
NNO.sub.2
oily substance
25 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NCH.sub.3 NSO.sub.2 CF.sub.3
oily substance
26 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NCH.sub.2 CHCH.sub.2
NCN oily substance
27 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NCH.sub.2 CCH
NCN oily substance
28 C.sub.2 H.sub.5
sec-C.sub.4 H.sub.9
(CH.sub.2).sub.2
NCOCH.sub.3
NCN oily substance
29 C.sub.2 H.sub.5
sec-C.sub.4 H.sub.9
(CH.sub.2).sub.2
NCH.sub.2 OCH.sub.3
NCN oily substance
__________________________________________________________________________
TABLE 1-4
__________________________________________________________________________
Comp. Physical
No. R.sup.1
R.sup.2
←A X Z Property
__________________________________________________________________________
30 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
##STR12##
NCH.sub.2 OC.sub.2 H.sub.5
NCN oily substance
31 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
##STR13##
NCH.sub.2 OC.sub.2 H.sub.5
NCN oily substance
32 C.sub.2 H.sub.5
sec-C.sub.4 H.sub.9
(CH.sub.2).sub.2
NSO.sub.2 N(CH.sub.3).sub.2
NCN oily substance
33 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NCH.sub.2 SCH.sub.3
NCN oily substance
34 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NCH.sub.3
NCOCF.sub.3
oily substance
35 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NC.sub.2 H.sub.5
C(CN).sub.2
oily substance
36 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
N-n-C.sub.3 H.sub.7
C(CN).sub.2
oily substance
37 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NH C(CN)COOC.sub.2 H.sub.5
oily substance
38 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NCH.sub.3
C(CN)COOC.sub.2 H.sub.5
oily substance
39 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NC.sub.2 H.sub.5
C(CN)COOC.sub.2 H.sub.5
oily substance
__________________________________________________________________________
TABLE 1-5
__________________________________________________________________________
Comp. Physical
No. R.sup.1
R.sup.2
←A
X Z Property
__________________________________________________________________________
40 C.sub.2 H.sub.5
sec-C.sub.4 H.sub.3
(CH.sub.2).sub.2
CH.sub.2 NCN oily substance
41 CH.sub.2
sec-C.sub.4 H.sub.3
(CH.sub.2).sub.2
NCH.sub.3 NCN m.p.: 76.0˜80.0° C.
42 C.sub.2 H.sub.5
CH.sub.3
(CH.sub.2).sub.2
NCH.sub.3 NCN m.p.: 116.0˜118.5° C.
43 C.sub.2 H.sub.5
C.sub.2 H.sub.5
(CH.sub.2).sub.2
NCH.sub.3 NCN oily substance
44 C.sub.2 H.sub.5
iso-C.sub.4 H.sub.3
##STR14##
NCH.sub.3 NCN oily substance
45 C.sub.2 H.sub.5
sec-C.sub.4 H.sub.3
CHCH.sub.2
O NCN oily substance
46 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NCOOC.sub.2 H.sub.5
NCN oily substance
47 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NCH.sub.2 CN NCN oily substance
48 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NSO.sub.2 CH.sub.3
NCN oily substance
49 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NCH.sub.2 OCH.sub.2 CH.sub.2 OCH.sub.3
NCN oily substance
50 C.sub.2 H.sub.5
sec-C.sub.4 H.sub.3
(CH.sub.2).sub.2
NCON(CH.sub.3).sub.2
NCN oily substance
__________________________________________________________________________
TABLE 1-6
__________________________________________________________________________
Comp. Physical
No. R.sup.1
R.sup.2
←A
X Z Property
__________________________________________________________________________
51 C.sub.2 H.sub.5
sec-C.sub.4 H.sub.3
(CH.sub.2).sub.2
N-n-C.sub.3 H.sub.7
NCN oily substance
52 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
NCH.sub.2 OCH.sub.3
NNO.sub.2
oily substance
53 C.sub.2 H.sub.5
sec-C.sub.4 H.sub.3
(CH.sub.2).sub.2
NCH.sub.2 OCH.sub.3
C(CN).sub.2
oily substance
54 C.sub.2 H.sub.5
sec-C.sub.4 H.sub.3
(CH.sub.2).sub.2
##STR15## C(CN).sub.2
oily substance
55 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
##STR16## NCN oily substance
56 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.3
NCH.sub.3 NCN m.p.: 58.5˜61.5° C.
57 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
CH.sub.2 NCN oily substance
58 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
CHCH.sub.3 NCN oily substance
59 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.2
CH.sub.2 NNO.sub.2
oily substance
60 C.sub.2 H.sub.5
n-C.sub.3 H.sub.7
(CH.sub.2).sub.3
CH.sub.2 NCN m.p.: 44.0˜47.0° C.
__________________________________________________________________________
TABLE 2-1
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
1 IR(KBr): 1251(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.1(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 C --H.sub.2 --C --H.sub.3), 2.7˜3.2(m, 2H,
SCH.sub.2), 3.0(s, 3H,
NCH.sub.3), 3.8˜4.5(m, 6H, OCH.sub.2, NCH.sub.2 CH.sub.2 N)
2 IR(neat): 1251(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.1(m, 11H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 C --H.sub.2 C --H.sub.3, NCH.sub.2 C --H.sub.3),
2.7˜3.75(m, 4H, SCH.sub.2,
NCH.sub.2), 3.8˜4.5(m, 6H, OCH.sub.2, NCH.sub.2 CH.sub.2 N)
3 IR(neat): 2176(C.tbd.N), 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.1(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 C --H.sub.2 --C -- H.sub.3), 2.7˜3.2(m, 2H,
SCH.sub.2), 3.3(s, 3H,
NCH.sub.3), 3.5˜4.5(m, 6H, OCH.sub.2, NCH.sub.2 CH.sub.2
______________________________________
N)
TABLE 2-2
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
4 IR(neat): 2176(C.tbd.N), 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.1(m, 11H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3, NCH.sub.2 C --H.sub.3),
2.7˜3.2(m, 2H, SCH.sub.2),
3.5˜4.5(m, 8H, OCH.sub.2, NCH.sub.2 CH.sub.2 N, NCH.sub.2)
5 IR(neat): 2170(C.tbd.N), 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.1(m, 13H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3, NCH.sub.2 C --H.sub.2 C
--H.sub.3), 2.7˜3.2(m, 2H,
SCH.sub.2), 3.4˜4.5(m, 8H, OCH.sub.2, NCH.sub.2 CH.sub.2 N,
NCH.sub.2)
6 IR(neat): 2170(C.tbd.N), 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.1(m, 15H, OCH.sub.2 C
-- .sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3, NCH.sub.2 C --H.sub.2 C
--H.sub.2 C --H.sub.3), 2.7˜3.2(m, 2H,
SCH.sub.2), 3.5˜4.5(m, 8H, SCH.sub.2, NCH.sub.2 CH.sub.2 N,
NCH.sub.2)
______________________________________
TABLE 2-3
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
7 IR(neat): 3232(NH), 2194(C.tbd.N), 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.1(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.7˜3.2(m, 2H,
SCH.sub.2), 3.4˜4.5(m,
6H, OCH.sub.2, NCH.sub.2 CH.sub.2 N), 8.00(bs, 1H, NH)
8 IR(neat): 3376(NH), 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.1(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 C --H.sub.2 C --H.sub.3), 2.36(s, 3H, ph-C --H.sub.3),
2.6˜3.1(m, 2H,
SCH.sub.2), 3.4˜4.4(m, 6H, OCH.sub.2, NCH.sub.2 CH.sub.2 N),
7.1˜7.9(m,
5H, NH, benzene)
9 IR(neat): 3370(NH), 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.1(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.7˜3.2(m, 2H,
SCH.sub.2), 2.93(s, 3H,
SO.sub.2 CH.sub.3), 3.5˜4.5(m, 6H, OCH.sub.2, NCH.sub.2
CH.sub.2 N), 7.34
(bs, 1H, NH)
______________________________________
TABLE 2-4
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
10 IR(neat): 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.1(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.7˜3.5(m, 4H,
SCH.sub.2, SC --H.sub.2 CH.sub.2 N),
2.99(s, 3H, SO.sub.2 CH.sub.3), 3.9˜4.5(m, 4H, OCH.sub.2,
SCH.sub.2 C --H.sub.2 N)
11 IR(neat): 2176(C.tbd.N), 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.1(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 C --H.sub.2 C --H.sub.3), 2.7˜4.7(m, 8H, SCH.sub.2,
SCH.sub.2 CH.sub.2 N,
OCH.sub.2)
12 IR(neat): 1251(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.1(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.7˜3.4(m, 4H,
SCH.sub.2, SC --H.sub.2 CH.sub.2 N),
4.0˜4.6(m, 4H, OCH.sub.2, SCH.sub.2 C --H.sub.2 N)
______________________________________
TABLE 2-5
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
13 IR(neat): 2176(C.tbd.N), 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.2(m, 13H, OCH.sub.2 C
--H.sub.3,
SCH--(C --H.sub.3)C --H.sub.2 C --H.sub.3, NCH.sub.2 C --H.sub.2
CH.sub.2 N), 3.1˜4.5(m, 7H,
SCH, OCH.sub.2, NC --H.sub.2 CH.sub.2 C --H.sub.2 N), 3.35(s, 3H,
NCH.sub.3)
14 IR(neat): 2182(C.tbd.N), 1266(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.1(m, 16H, OCH.sub.2 C
--H.sub.3,
OCH.sub.2 --C --H.sub.3, SCH.sub.2 C --H.sub.2 C --H.sub.3,
SCH.sub.2 C --H.sub.2 C --H.sub.3), 2.6˜3.2
(m, 4H, SCH.sub.2, SCH.sub.2), 3.9˜4.5(m, 8H, OCH.sub.2,
OCH.sub. 2,
NCH.sub.2 CH.sub.2 N)
15 IR(neat): 2176(C.tbd.N), 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 17H, OCH.sub.2 C
--H.sub.3,
SCH--(C --H.sub.3)C --H.sub.2 C --H.sub.3, N--CH(C --H.sub.3).sub.2)
, 3.2˜4.5(m, 7H,
SCH, NCH.sub.2 --CH.sub.2 N, OCH.sub.2), 4.7˜5.2(m, 1H,
______________________________________
NCH)
TABLE 2-6
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
16 IR(neat): 2176(C.tbd.N), 1254(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 11H, OCH.sub.2 C
--H.sub.3,
SCH--(C --H.sub.3)C --H.sub.2 C --H.sub.3), 3.20˜4.5(m, 7H,
SCH,
NCH.sub.2 CH.sub.2 N, OCH.sub.2), 3.32(s, 3H, NCH.sub.3)
17 IR(neat): 2200(C.tbd.N), 1263(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.1˜3.7(m, 8H,
NCH.sub.2 CH.sub.2 CH.sub.2 N,
SCH.sub.2), 3.35(s, 3H, NCH.sub.3), 3.9˜4.5(m, 2H,
OCH.sub.2)
18 IR(neat): 2200(C.tbd.N), 1269(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub. 3), 2.6˜4.5(m, 8H,
SCH.sub.2, NCH.sub.2 CH.sub.2 N,
OCH.sub.2), 3.30(s, 3H, NCH.sub.3)
______________________________________
TABLE 2-7
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
19 IR(neat): 1617(C═N)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.6˜4.5(m, 8H,
SCH.sub.2, NCH.sub.2 CH.sub.2 N,
OCH.sub.2), 2.97(s, 3H, SO.sub.2 CH.sub.3), 3.30(s, 3H,
______________________________________
NCH.sub.3)
TABLE 2-8
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
20 IR(KBr): 2200(C.tbd.N), 1265(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 11H, OCH.sub.2 C
--H.sub.3,
SCH--(C --H.sub.3)C --H.sub.2 C --H.sub.3), 3.20˜4.5(m, 7H,
SCH,
NCH.sub.2 CH.sub.2 N, OCH.sub.2), 3.30(s, 3H, NCH.sub.3)
21 IR(neat): 3274(NH), 1248(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.56(s, 3H, NCH.sub.3),
2.70˜3.20(m, 2H,
SCH.sub.2), 3.9˜4.7(m, 6H, OCH.sub.2, NCH.sub.2 N, NCH.sub.2
N), 9.49
(bs, 1H, NH)
22 IR(neat): 1248(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C -- H.sub.3), 2.58(s, 3H, NCH.sub.3),
3.0(s, 3H, NCH.sub.3),
2.70˜3.2(m, 2H, SCH.sub.2), 3.8˜4.5(m, 6H, NCH.sub.2
N,
NCH.sub.2 N)
______________________________________
TABLE 2-9
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
24 IR(neat): 1572(C=N), 1251(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.7˜3.2(m, 2H,
SCH.sub.2), 3.7˜4.5(m,
8H, OCH.sub.2, NC --H.sub.2 CH═CH.sub.2, NCH.sub.2 CH.sub.2 N),
5.1˜6.0(m,
3H, NCH.sub.2 C --H═C --H.sub.2)
25 IR(neat): 1515(C=N), 1248(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.7˜3.2(m, 2H,
SCH.sub.2), 3.13(s, 3H,
NCH.sub.3) 3.6˜4.5(m, 6H, OCH.sub.2, NCH.sub.2 CH.sub.2 N)
26 IR(neat): 2176(C.tbd.N), 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.7˜3.2(m, 2H,
SCH.sub.2), 3.6˜4.5(m,
8H, OCH.sub.2, NC --H.sub.2 CH═CH.sub.2, NCH.sub.2 CH.sub.2 N),
5.1˜6.0(m,
3H, NCH.sub.2 C --H═C --H.sub.2)
______________________________________
TABLE 2-10
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
27 IR(neat): 3232(C.tbd.CH), 2182(C.tbd.N), 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.38(t, 1H, CH.sub.2 CH.tbd.C
--H), 2.7˜3.2
(m, 2H, SCH.sub.2), 3.6˜4.5(m, 6H, OCH.sub.2, NCH.sub.2
CH.sub.2 N),
5.55(d, 2H, NC --H.sub.2 C.tbd.CH)
28 IR(neat): 2188(C.tbd.N), 1737(C=O), 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 11H, OCH.sub.2 C
--H.sub.3,
SCH--(C --H.sub.3)C --H.sub.2 C --H.sub.3), 2.54(s, 3H, COC
--H.sub.3), 3.2˜4.7
(m, 7H, SCH, NCH.sub.2 CH.sub.2 N, OCH.sub.2)
29 IR(neat): 2182(C.tbd.N), 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 11H, OCH.sub.2 C
--H.sub.3,
SCH--(C --H.sub.3)C --H.sub.2 C --H.sub.3), 3.2˜4.5(m, 7H,
SCH,
NCH.sub.2 CH.sub.2 N, OCH.sub.2), 3.41(s, 3H, CH.sub.3 O), 5.11(s,
2H,
NCH.sub.2 O)
______________________________________
TABLE 2-11
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
30 IR(neat): 2182(C.tbd.N), 1260(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 14H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3, OCH.sub.2 C --H.sub.3, NCH(C
--.sub.3)CH.sub.2 N),
2.7˜4.5(m, 9H, SCH.sub.2, OCH.sub.2, OCH.sub.2,
NC --H(CH.sub.3)C --H.sub.2 N),
5.14(s, 2H, NCH.sub.2 O)
31 IR(neat): 2176(C.tbd.N), 1272(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 17H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3, OCH.sub.2 C --H.sub.3,
NCH.sub.2 C(C --H.sub.3).sub.2 CH.sub.2 N),
2.6˜4.5(m, 10H, SCH.sub.2, OCH.sub.2, OCH.sub.2,
NC --H.sub.2 C(CH.sub.3).sub.2 C --H.sub.2 N), 5.16(s, 2H,
NCH.sub.2 O)
32 IR(neat): 2188(C.tbd.N), 1263(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 11H, OCH.sub.2 C
--H.sub.3,
SCH--(C --H.sub.3)C --H.sub.2 C --H.sub.3), 2.95(s, 6H, SO.sub.2
N(CH.sub.3).sub.2),
3.2˜4.5(m, 7H, SCH, NCH.sub.2 CH.sub.2 N, OCH.sub.2)
______________________________________
TABLE 2-12
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
33 IR(neat): 2176(C.tbd.N), 1266(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.25(s, 3H, SCH.sub.3),
2.7˜3.2(m, 2H,
SCH.sub.2), 3.6˜4.5(m, 6H, NCH.sub.2 CH.sub.2 N, OCH.sub.2),
4.90(s, 2H,
SCH.sub.2 N)
34 IR(neat): 1662(C=N), 1599(C=N), 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.6˜3.2(m, 2H,
SCH.sub.2), 2.91(s, 3H,
NCH.sub.3), 3.6˜4.5(m, 6H, NCH.sub.2 CH.sub.2 N, OCH.sub.2)
35 IR(neat): 2200(C.tbd.N), 1263(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 11H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3, NCH.sub.2 C --H.sub.3),
2.6˜3.2(m, 2H, SCH.sub.2),
3.5˜4.5(M, 8H, NCH.sub.2, NCH.sub.2 CH.sub.2 N,
______________________________________
OCH.sub.2)
TABLE 2-13
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
36 IR(neat): 2200(C.tbd.N), 1265(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 13H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3, NCH.sub.2 C --H.sub.2 C
--H.sub.3), 2.6˜3.2(m, 2H,
SCH.sub.2), 3.5˜4.5(m, 8H, NCH.sub.2, NCH.sub.2 CH.sub.2 N,
OCH.sub.2)
37 IR(neat): 3292(NH), 2200(C.tbd.N), 1671(C=O),
1254(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 11H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3, COOCH.sub.2 C --H.sub.3),
2.6˜3.2(m, 2H, SCH.sub.2),
3.5˜4.5(m, 8H, NCH.sub.2 CH.sub.2 N, COOC --H.sub.2 CH.sub.3,
OCH.sub.2),
9.43(bs, 1H, NH)
38 IR(neat): 2188(C.tbd.N), 1686(C=O), 1257(P=O)cm.sup. -1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 11H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3, COOCH.sub.2 C --H.sub.3),
2.6˜3.2(m, 2H, SCH.sub.2),
3.15(s, 3H, NCH.sub.3), 3.4˜4.5(m, 8H, NCH.sub.2 CH.sub.2 N,
COOC --H.sub.2 --CH.sub.3, OCH.sub.2)
______________________________________
TABLE 2-14
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
39 IR(neat): 2188(CN), 1686(CO),
1257(PO)cm.sup.-1 NMR(CDCl.sub.3), δ(ppm):
0.8˜2.0(m, 14H, OCH.sub.2 C --H.sub.3,
SCH.sub.2 C --H.sub.2 C --H.sub.3, NCH.sub.2 C --H.sub.3,
COOCH.sub.2 C --H.sub.3), 2.6˜3.2(m, 2H, SCH.sub.2),
3.4˜4.5(m, 10H, NCH.sub.2 CH.sub.2 N, NCH.sub.2,
COOC --H.sub.2 CH.sub.3, OCH.sub.2)
40 IR(neat): 2188(CN), 1608(CN),
1254(PO)cm.sup.-1 NMR(CDCl.sub.3), δ(ppm):
0.8˜2.3(m, 13H, OCH.sub.2 C --H.sub.3, SCH
##STR17##
41 IR(KBr): 2176(CN), 1254(PO)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H,
SCH(C --H.sub.3)
C --H.sub.3 C --H.sub.3),
3.32(s, 3H, NCH.sub.3), 3.2˜3.9(m, 5H, SCH, NCH.sub.2
CH.sub.2 N),
3.81(d, 3H, OCH.sub.3)
______________________________________
TABLE 2-15
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
42 IR(KBr): 2176(C.tbd.N), 1254(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 1.35(t, 3H, OCH.sub.2 C --H.sub.3),
2.40(d,
3H, SCH.sub.3), 3.32(s, 3H, NCH.sub.3), 3.6˜4.5(m, 6H, N--
CH.sub.2 CH.sub.2 N, OCH.sub.2)
43 IR(neat): 2176(C.tbd.N), 1254(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 1.35(t, 6H, OCH.sub.2 C --H.sub.3,
SCH.sub.2 C --H.sub.3), 2.6˜3.2(m, 2H, SCH.sub.2), 3.32(s,
3H, NCH.sub.3),
3.6˜4.5(m, 6H, NCH.sub.2 CH.sub.2 N, OCH.sub.2)
44 IR(neat): 2176(C.tbd.N), 1260(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.9˜2.1(m, 10H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 -- --CH(C --H.sub.3).sub.2), 2.7˜3.1(m, 2H,
SCH.sub.2), 3.32(s, 3H,
NCH.sub.3), 3.6˜4.5(m, 6H, NCH.sub.2 CH.sub.2 N,
______________________________________
OCH.sub.2)
TABLE 2-16
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
45 IR(neat): 2212(C.tbd.N), 1260(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 14H, OCH.sub.2 C
--H.sub.3,
SCH--(C --H.sub.3)C --H.sub.2 C --H.sub.3, OC .sub.--H(C --H.sub.3)
CH.sub.2 N),
3.2˜4.5(m, 5H, SCH, OCH(CH.sub.3)C --H.sub.2 N, OCH.sub.2),
4.8˜5.4(m, 1H, OC --H(CH.sub.3)CH.sub.2 N)
46 IR(neat): 2194(C.tbd.N), 1764(C=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 11H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3, COOCH.sub.2 C --H.sub.3),
2.72˜3.26(m, 2H,
SCH.sub.2), 3.8˜4.5(m, 8H, NCH.sub.2 CH.sub.2 N, OCH.sub.2,
COOC --H.sub.2 CH.sub.3)
47 IR(neat): 2182(C.tbd.N), 1260(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.70˜3.22(m, 2H,
SCH.sub.2), 3.6˜4.5
(m, 6H, NCH.sub.2 CH.sub.2 N, OCH.sub.2), 4.62(s, 2H, NCH.sub.2
______________________________________
CN)
TABLE 2-17
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
48 IR(neat): 2188(C.tbd.N), 1260(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.6˜3.2(m, 2H,
SCH.sub.2), 3.45(s, 3H,
SO.sub.2 CH.sub.3) 3.6˜4.5(m, 6H, NCH.sub.2 CH.sub.2 N,
OCH.sub.2)
49 IR(neat): 2182(C.tbd.N), 1257(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.7˜3.2(m, 2H,
SCH.sub.2), 3.35(s, 3H,
OCH.sub.3), 3.4˜4.5(m, 10H, NCH.sub.2 CH.sub.2 N, OCH.sub.2
CH.sub.2 O,
OC --H.sub.2 CH.sub.3), 5.20(s, 2H, OCH.sub.2 N)
______________________________________
TABLE 2-18
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
50 IR(neat): 2182(C.tbd.N), 1710(C=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 11H, OCH.sub.2 C
--H.sub.3,
SCH--(C --H.sub.3)C --H.sub.2 C --H.sub.3), 3.05 (s, 6H,
N(CH.sub.3).sub.2), 3.2˜4.5
(m, 7H, SCH, NCH.sub.2 CH.sub.2 N, OCH.sub.2)
51 IR(neat): 2176(C.tbd.N), 1253(P=O).sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 16H, OCH.sub.2 C
--H.sub.3,
SCH--(C --H.sub.3)C --H.sub.2 C --H.sub.3, NCH.sub.2 C --H.sub.2 C
--H.sub.3), 3.2˜4.5(m, 9H,
SCH, NCH.sub.2 CH.sub.2 N, NCH.sub.2, OCH.sub.2)
52 IR(neat): 1563(C=B), 1248(P=O)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 2.7˜4.5(m, 8H,
SCH.sub.2, NCH.sub.2 CH.sub.2 N,
OCH.sub.2), 3.32(s, 3H, OCH.sub.3), 4.70(s, 2H, OCH.sub.2 N)
______________________________________
TABLE 2-19
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
53 IR(neat): 2206(C.tbd.N), 1560(C=C)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 11H, OCH.sub.2 C
--H.sub.3,
SCH--(C --H.sub.3)C --H.sub.2 C --H.sub.3), 3.2˜4.5(m, 7H,
SCH,
NCH.sub.2 CH.sub.2 N, OCH.sub.2), 3.39(s, 3H, OCH.sub.3), 5.01(s,
2H,
OCH.sub.2 N)
54 IR(neat): 2212(C.tbd.N), 1719(C=O), 1563(C=C)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 17H, OCH.sub.2 C
--H.sub.3,
SCH--(C --H.sub.3)C --H.sub.2 C --H.sub.3, NCOC(CH.sub.3).sub.2),
3.2˜3.8(m, 3H,
SCH, CH.sub.2 Cl), 4.0˜4.5(m, 6H, OCH.sub.2, NCH.sub.2
CH.sub.2 N)
55 IR(neat): 2176(C.tbd.N), 1722(C=O), 1617(C=N)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.0(m, 8H, OCH.sub.2 C
--H.sub.3,
SCH.sub.2 --C --H.sub.2 C --H.sub.3), 1.21(s, 9H,
C(CH.sub.3).sub.3), 2.7˜4.8(m, 10H,
OCH.sub.2, SCH.sub.2, NCH.sub.2 CH.sub.2 N, NCH.sub.2 CO)
______________________________________
TABLE 2-20
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
56 IR(neat): 2170(CN), 1590(CN)
cm.sup.-1 NMR(CDCl.sub.3), δ(ppm): 0.8˜2.2(m, 10H,
OCH.sub.2
C --H.sub.3, SCH.sub.2 C --H.sub.2 C --H.sub.3,
NCH.sub.2 C --H.sub.2 CH.sub.2 N), 2.6˜4.5(m, 8H,
SCH.sub.2),
OCH.sub.2, NC --H.sub.2 CH.sub.2 C --N), 3.37(s, 3H, NCH.sub.3)
57 IR(neat): 2188(CN), 1608(CN),
1257(PO)cm.sup.-1 NMR(CDCl.sub.3), δ(ppm):
0.8˜2.4(m, 10H, OCH.sub.2 C --H.sub.3, SCH
##STR18##
58 IR(neat): 2188(CN), 1605(CN),
1257(PO)cm.sup.-1 NMR(CDCl.sub.3), δ(ppm):
0.8˜3.4(m, 16H, OCH.sub.2 C --H.sub.3 SCH.sub.2
##STR19##
______________________________________
TABLE 2-21
______________________________________
Comp.
No. IR Spectra and NMR Spectra
______________________________________
59 IR(neat): 1542(CN), 1263(PO)cm.sup.-1
NMR(CDCl.sub.3), δ(ppm): 0.8˜2.4(m, 10H, OCH.sub.2
C --H.sub.3, SCH.sub.2
##STR20##
60 IR(neat): 2182(CN), 1563(CN),
1254(PO)cm.sup.-1 NMR(CDCl.sub.3), δ(ppm):
0.8˜2.1(m, 12H, OCH.sub.2 C --H.sub.3,SCH.sub.2
##STR21##
______________________________________
The compounds of the present invention exhibit excellent activity as active ingredients of insecticides, acaricides and nematocides. The compounds of the present invention are effective for controlling, for instance, agricultural and horticultural pests such as Coleoptera (for instance, Scarabaeidae, Chrysomelidae, Henosepilachna vigintioctopunctate and Lissorhoptrus oryzophilus), Lepidoptera (for instance, Mamestra brassicae, Pieris rapae, Plutera xylostella, Noctuidae, Adoxophyes orana and Chilo suppressalis), Hemiptera (for instance, Delphacidae, Deltocephalidae, Aleyrodidae, Aphididae and Scales) and Thysanoptera (for instance, Scirtothrips dorsalis and Thrips pulmi); Sanitary pests such as Mosquitoes, Flies, Blattidae, Fleas and Lice; Grain pests; cloth and house pests; Plant parasitic nematodes such as root-knot nematodes and root-lesion nematodes; and Plant parasitic mites such as Tetranychus urticae, Tetranychus cinnabarinus, Tetranychus kanzawai and Panonychus citri. They are also effective for controlling soil insect pests. The term "soil insect pest" used herein means, for instance, Gastropoda such as slugs and snails; Isopoda such as Armadillidium vulgare and Sow bugs. In addition, they are likewise effective for controlling insect pest such as Dicofol, organophosphorus compound-resistant plant parasitic mites, organophosphorus compound-resistant Aphididae and Musca domestica.
When the compounds of the present invention are used as active ingredients of insecticidal, acaricidal, nematocidal compositions and composition for killing or controlling soil pest insect, they may be used as such, but may in general be formed into a variety of formulations together with adjuvants such as emulsifiable concentrates, dusts, wettable powders, liquid formulations, aerosols and pastes like conventional formulations of agricultural chemicals. The formulations in general comprise 0.5 to 90 parts by weight of the active ingredient and 10 to 99.5 parts by weight of an adjuvant. When these formulations are practically used, they can be applied as such or after diluting them with a diluent such as water to a desired concentration.
The term "adjuvant" herein means carriers, emulsifying agents, suspending agents, dispersing agents, spreaders, penetrants, wetting agents, thickeners and stabilizers. These adjuvants may, if necessary, be added in an appropriate amount. The carriers can roughly be classified into solid carriers and liquid carriers. Examples of the solid carriers include vegetable and animal powder such as starches, active carbon, soybean flour, wheat flour, wood powder, fish meal and powdered milk; and mineral powders such as talc, kaolin, bentonite, calcium carbonate, zeolite, diatomaceous earth, white carbon, clay, alumina and powdered sulfur. On the other hand, examples of the liquid carriers are water; alcohols such as methyl alcohol and ethylene glycol; ketones such as acetone and methyl ethyl ketone; ethers such as dioxane and tetrahydrofuran; aliphatic hydrocarbons such as kerosine; aromatic hydrocarbons such as xylene, trimethylbenzene, tetramethylbenzene, cyclohexane and solvent naphtha; halogenated hydrocarbons such as chloroform and chlorobenzene; amides such as dimethylformamide; esters such as ethyl acetate and glycerin esters of fatty acids; nitriles such as acetonitrile; and sulfur atom-containing compounds such as dimethylsulfoxide. If necessary, the compounds of the present invention may be admixed with or used simultaneously with other agricultural chemicals such as insecticides, acaricides, nematocides, bactericides, antiviral agents, attractants, herbicides and plant growth regulators. In admixtures, greater effectiveness may sometimes be attained.
Examples of insecticides, acaricides or nematocides include organophosphorus acid ester compounds such as DDVP, Diazinon, Malathion, Fenitrothion, Prothiofos, Dioxabenzofos and Acephate; carbamate compounds such as Carbaryl, Propoxur, Oxamyl, Carbofuran and Methomyl; organochlorine compounds such as Dicofol and Tetradifon; organometal compounds such as Cyhexatin and Fenbutatin oxide; pyrethroid compounds such as Fenvalerate, Permethrin, Deltamethrin and Bifenthrin; urea compounds such as Diflubenzuron, Teflubenzuron and Chlorfluazuron; heterocyclic compounds such as Buprofezin and Hexythiazox; and other compounds such as dinitro compounds, organosulfur compounds, amidine compounds and triazine compounds. In addition to the foregoing compounds, the compound of the present invention can also be admixed with or used simultaneously with microbial pesticides such as BT agents and insect pathogen virus pesticides.
Examples of the bactericides are organophosphorus compounds such as Iprobenfos, Edifenphos and Phosethyl-aluminum; organocopper compounds such as oxyguinoline copper, copper terephthalate; organochlorine compounds such as Fthalide and Chlorothalonil; dithiocarbamate compounds such as Maneb, Zineb and Propineb; dicarboximide compounds such as Iprodione, Vinclozolin and Procymidone; azole compounds such as Triadimefon, Bitertanol, Etaconazole, Propiconazole and Penconazole; benzimidazole compounds such as Thiophanate-methyl and Benomyl; carbinol compounds such as Fenarimol and Flutriafol; benzanilide compounds such as Mepronil and Flutolanil; phenylamide compounds such as Metalaxyl and Oxadixyl; and other compounds such as piperazine compounds, quinoxaline compounds, morpholine compounds, anthraquinone compounds, sulfenic acid compounds, crotonic acid compounds, urea compounds and antibiotics.
As has been discussed above, the insecticides, acaricides and nematocides which comprise, as active ingredient, the compounds of the present invention are effective for controlling a variety of deleterious insects, harmful mites, destructive nematodes and harmful soil insect pests. These agricultural chemicals or formulations are applied at a concentration ranging from 1 to 20,000 ppm, desirably 20 to 2,000 ppm expressed in terms of the amount of the active ingredient. The concentration of these active ingredients can be appropriately adjusted depending on various factors such as shapes of the formulations, methods, purposes, time and places of application as well as the condition of infestation of insect pest. For instance, when aquatic insect pests are to be controlled, the insect pest can be controlled by spraying a solution of the compound having a concentration falling within the range defined above and, therefore, the concentration of the active ingredient required for controlling the aquatic insect pest is lower than that defined above. The amount of the agricultural chemicals or formulations to be applied per unit area (per 10 a) ranges from about 0.1 to 5,000 g and preferably 10 to 1,000 g expressed in terms of the amount of the active ingredient, but in a particular case, they may be applied in an amount outside the range defined above.
The application of a variety of formulations or dilute solutions thereof which comprise the compounds of the present invention can be performed according to any manner of application usually adopted, for instance, spraying (such as spraying, dusting, misting, atomizing, granule application and application on water surface); soil applications (such as mixing and drench); surface applications (such as coating, dressing and painting); and poison bait. It is also possible to control the development and growth of harmful insect pests, in particular deletrious insects through the action of excreta obtained by admixing the foregoing active ingredient to feed and giving the feed to domestic animals. Further, they can also be applied in accordance with ultra low volume application. In this method, the chemicals or formulations can comprise 100% active ingredient.
The method for preparing the compounds of the present invention will hereinafter be explained in more detail with reference to the following Preparation Examples.
2.00 g of O-ethyl-S-n-propyl-(2-nitroimino-1-imidazolidinyl)phosphonothiolate was dissolved in 20 ml of N,N-dimethylformamide and then 0.32 g of a 60% sodium hydride was gradually added to the resulting solution. Thereafter, the solution was cooled down to 0° to 5° C. and 1.27 g of ethyl iodide was gradually added thereto dropwise. After the completion of the dropwise addition, the temperature of the solution was slowly brought back to room temperature and the solution was further stirred for additional 12 hours to complete the reaction. After the reaction, the solution was poured into ice water and extracted with dichloromethane. The dichloromethane phase was washed with water, dried over anhydrous magnesium sulfate, the dichloromethane was distilled off under reduced pressure and the residue obtained was purified by silica gel column chromatography (eluent: ethyl acetate) to give 0.50 g of Compound No. 2 as an oily substance.
To a mixture comprising 0.44 g of a 60% sodium hydride and 50 ml of N,N-dimethylformamide, 1.24 g of 1-methyl-2-cyanoiminoimidazolidine was gradually added. After the mixture was allowed to stand for a brief period, 2.76 g of an 88.2% toluene solution of O-ethyl-S-n-propylphosphorochloride thiolate was gradually dropwise added to the mixture. After the completion of the dropwise addition, the reaction solution was poured into ice water and then extracted with chloroform. The chloroform phase was washed with water, dried over anhydrous magnesium sulfate, the chloroform was distilled off under reduced pressure and the residue obtained was purified by silica gel column chromatography (eluent: chloroform/methanol=97:3) to give 1.50 g of Compound No. 3 as an oily substance.
2.0 g of 2-methanesulfonyliminoimidazolidine was dissolved in 20 ml of N,N-dimethylformamide. The resulting solution was cooled down to 0° C. and then 1.02 g of a 60% sodium hydride was gradually added. Thereafter, 3.00 g of an 88.2% toluene solution of O-ethyl-S-n-propylphosphorochloride thiolate was gradually dropwise added to the solution. After the completion of the dropwise addition, the temperature of the reaction solution was slowly brought back to room temperature and further the reaction was continued for additional 12 hours. After the reaction, the reaction solution was poured into ice water, neutralized with a 10% hydrochloric acid solution and then extracted with chloroform. The chloroform phase was washed with water, dried over anhydrous magnesium sulfate, the chloroform was distilled off under reduced pressure and the residue obtained was purified by silica gel column chromatography (eluent: chloroform/methanol=97:3) to give 2.20 g of Compound No. 9 as an oily substance.
1.50 g of O-ethyl-S-sec-butyl-(2-cyanoimino-1-imidazolidinyl)phosphonothiolate was dissolved in 20 ml of tetrahydrofuran. The resulting solution was cooled and maintained at a temperature of ranging from 0° to 5° C. and 0.25 g of a 60% sodium hydride was gradually added to the solution. After 30 minutes, 0.50 g of chloromethyl methyl ether was dropwise added thereto. After the completion of the dropwise addition, the temperature of the reaction solution was brought back to room temperature and the solution was stirred for additional 3 hours to complete the reaction.
After the reaction, the reaction solution was poured into ice water and then extracted with ethyl acetate. The ethyl acetate phase was washed with water, dried over anhydrous magnesium sulfate, the ethyl acetate was distilled off under reduced pressure and the residue obtained was purified by silica gel column chromatography (eluent: chloroform) to thus give 1.10 g of Compound No. 29 as an oily substance.
Specific examples of formulations will be described below, but the adjuvants such as carriers and surfactants are by no means limited to those used in the following examples. In the following specific formulations, the term "part" means "part by weight" unless otherwise specified.
20 parts of Compound No. 1, 56 parts of acid clay, 15 parts of white carbon, 4 parts of calcium lignin sulfonate and 5 parts of polyoxyethylene alkylphenyl ether were uniformly mixed and pulverized to give a wettable powder.
To 20 parts of Compound No. 2, 75 parts of xylene was added. And then, 5 parts of New Calgen ST-20 (available from Takemoto Oil & Fat Co., Ltd.) was added to the resulting solution as an emulsifying agent and then the mixture was mixed and dissolved to give an emulsifiable concentrate.
5 parts of Compound No. 1, 3 parts of calcium lignin sulfonate, one part of sodium dodecylbenzenesulfonate, 30 parts of bentonite and 61 parts of clay were sufficiently pulverized and mixed. The mixture was then sufficiently kneaded while adding water, followed by granulation and drying to thus give a granule.
The insecticidal, acaricidal and nematocidal effects of the compounds of the present invention will hereunder be explained with reference to the following Test Examples.
The emulsifiable concentrate obtained by Formulation Example 2 was diluted with water to 500 ppm and 50 ppm and the resulting diluted emulsions were sprayed on leaves of chinese cabbage. After air-drying, the leaves were introduced into a plastic container having a size of 21 cm (height)×13 cm (width)×3 cm (depth), then 10 third instar larvae of common cutworm were put on the leaves. The container was then placed in a thermostated room maintained at 26° C. After 2 days, the number of surviving larvae was recorded to obtain the mortality (%) (repeated two times). The results thus obtained are summarized in the following Table 3.
TABLE 3
______________________________________
Concn. of
Compound No.
Active Ingredient (ppm)
Mortality (%)
______________________________________
2 500 100
50 0
3 500 100
50 70
4 500 100
50 70
5 500 100
50 90
6 500 100
50 100
7 500 100
50 100
9 500 100
50 80
10 500 100
50 0
14 500 100
50 100
15 500 100
50 90
16 500 100
50 20
17 500 100
50 60
18 500 100
50 100
20 500 100
50 90
21 500 100
50 0
26 500 100
50 10
27 500 100
50 0
29 500 100
50 20
30 500 100
50 100
31 500 100
50 50
32 500 100
50 10
33 500 100
50 70
34 500 100
50 100
35 500 100
50 80
36 500 100
50 20
37 500 100
50 90
38 500 100
50 50
39 500 100
50 40
40 500 100
50 0
41 500 100
50 100
44 500 100
50 90
45 500 100
50 90
46 500 100
50 100
47 500 100
50 50
49 500 100
50 0
50 500 100
50 10
51 500 100
50 50
53 500 100
50 10
Comparative
500 100
Compound A 50 10
Untreated -- 0
______________________________________
The Comparative Compound A as set forth in Table 3 is a compound represented by the following structural formula and disclosed in Japanese Unexamined Patent Publication No. Sho 61-267594: ##STR22##
The emulsifiable concentrate obtained by Formulation Example 2 was diluted with water to 500 ppm and the seedlings of rice plant were immersed therein for 10 seconds. After air-drying, the seedlings whose roots were wrapped round with absorbent cotton were introduced into a test tube, then 10 second instar larvae of green rice leafhopper were put into the test tube, the opening thereof was closed with gauze. The tube was placed in a thermostated room maintained at 26° C. After 2 days, the number of surviving larvae was recorded to obtain the mortality (%) (repeated two times). The results thus obtained are summarized in the following Table 4.
TABLE 4
______________________________________
Concn. of
Compound No.
Active Ingredient (ppm)
Mortality (%)
______________________________________
1 500 100
3 500 100
4 500 100
5 500 100
9 500 100
10 500 100
11 500 100
14 500 100
15 500 100
16 500 100
17 500 100
18 500 100
19 500 100
20 500 100
21 500 100
26 500 100
27 500 100
28 500 100
29 500 100
30 500 100
31 500 100
32 500 100
33 500 100
34 500 100
35 500 100
37 500 100
38 500 100
40 500 100
41 500 100
44 500 100
45 500 100
46 500 100
47 500 100
49 500 100
50 500 100
51 500 100
53 500 100
Comparative
500 100
Compound A
Untreated -- 0
______________________________________
The comparative Compound A as set forth in Table 4 is the same as that defined above in connection with Table 3.
A kidney bean leaf was cut into 3×5 cm2. The leaf was put on a filter paper wetted with water for preventing drying of the leaf and 20 female adults of kanzawa spider mite were released on the leaf. After 24 hours, 500 ppm and 50 ppm of concentration of active ingredient prepared by diluting with water the emulsifiable concentrate obtained by Formulation Example 2 were sprayed on the leaf. After air-drying, the mites were held in a thermostated room maintained at 26° C. After 24 hours, the number of surviving adults were recorded to obtain the mortality (%) (repeated two times). The results thus obtained are summarized in the following Table 5.
TABLE 5
______________________________________
Concn. of
Compound No.
Active Ingredient (ppm)
Mortality (%)
______________________________________
1 500 100
50 0
2 500 100
50 0
3 500 100
50 80
4 500 100
50 20
5 500 100
50 40
6 500 100
50 50
7 500 100
50 90
9 500 100
50 60
10 500 100
50 70
11 500 100
50 80
12 500 100
50 0
14 500 100
50 80
15 500 100
50 10
16 500 100
50 0
17 500 100
50 30
18 500 100
50 90
19 500 100
50 0
20 500 100
50 0
26 500 100
50 30
27 500 100
50 20
28 500 100
50 30
29 500 100
50 50
30 500 100
50 20
31 500 100
50 10
32 500 100
50 0
33 500 100
50 0
34 500 100
50 20
35 500 100
50 10
36 500 100
50 10
37 500 100
50 50
38 500 100
50 20
39 500 100
50 0
40 500 100
50 10
41 500 100
50 80
44 500 100
50 10
45 500 100
50 10
46 500 100
50 20
47 500 100
50 20
50 500 100
50 0
51 500 100
50 10
53 500 100
50 0
Comparative
500 100
Compound A 50 10
Untreated -- 0
______________________________________
The Comparative Compound A is the same as that defined above in connection with Table 3.
To a 1/5,000 are pot, soil contaminated with root-knot nematodes was packed and the soil was admixed with the granules obtained by Formulation Example 3 in an amount of 250 g and 25 g/are expressed in terms of the amount of the active ingredient. Two days after the treatment, seedlings of tomato at 3rd to 4th-leaf stage were transplanted in the soil. Twenty-five days after the transplantation, the degree of the invasion of root-knot nematodes (root-knot index) was determined (repeated two times).
The root-knot index was evaluated on the basis of the following evaluation criteria:
______________________________________ 0 no invasion of root-knot nematodes 1 slight invasion of root-knot nematodes 2 medium invasion of root-knot nematodes 3 severe invasion of root-knot nematodes 4 very severe invasion of root-knot nematodes ______________________________________
The results thus obtained are summarized in the following Table 6.
TABLE 6
______________________________________
Compound Amount of Active Ingredient
No. (g/are) Root-Knot Index
______________________________________
1 250 0
25 3
2 250 0
25 2
3 250 0
25 0
4 250 0
25 0
5 250 0
25 1
6 250 0
25 3
7 250 0
25 1
8 250 0
25 2
9 250 0
25 0
10 250 0
25 2
12 250 0
25 3
14 250 0
25 0
15 250 0
25 0
16 250 0
25 1
17 250 0
25 0
18 250 0
25 0
20 250 0
25 0
21 250 0
25 3
25 250 0
25 3
26 250 0
25 0
27 250 0
25 0
29 250 0
25 0
30 250 0
25 0
31 250 0
25 0
33 250 0
25 2
34 250 0
25 0
35 250 0
25 0
36 250 0
25 2
37 250 0
25 0
38 250 0
25 0
39 250 0
25 0
40 250 0
25 0
41 250 0
25 0
43 250 0
25 3
44 250 0
25 0
45 250 0
25 3
47 250 0
25 3
49 250 0
25 2
50 250 0
25 0
51 250 0
25 0
53 250 0
25 0
54 250 0
25 1
Comparative
250 0
Compound A
25 2
Comparative
250 0
Compound B
25 1
Untreated
-- 4
______________________________________
The comparative Compound A as set forth in Table 6 is the same as that defined above in connection with Table 3 and Comparative Compound B is a compound (oxamyl) represented by the following structural formula: ##STR23##
The compounds of the present invention represented by the foregoing general formula (I) exhibit effectiveness in controlling harmful insects, mites and nematodes and thus can be used as novel insecticides, acaricides and nematocides which do not give off a bad or irritating odor and have low toxicity to warm-blooded animals.
Claims (20)
1. An organophosphorus compound represented by formula (I) ##STR24## wherein R1 and R2 each represent C1 to C4 alkyl;
X represents NH or N--R4, wherein R4 represents C1 to C4 alkyl; C1 to C4 alkyl substituted with at least one group selected from the group consisting of alkoxy, alkylthio, cyano, alkoxyalkyloxy, alkylamino and halogen; alkenyl; halogen substituted alkenyl; alkynyl; halogen substituted alkynyl; phosphoric acid ester; cyano; a group of formula II: ##STR25## (wherein R5 represents alkyl, halogen substituted alkyl, alkylamino, or halogen substituted alkylamino); or --(R6) n --CO-- R7 (wherein n is 0 or 1; R6 represents methylene, alkyl substituted methylene, ethylene and alkyl substituted ethylene; and R7 represents alkyl, halogen substituted alkyl, alkoxy, halogen substituted alkoxy, alkylthio, alkylamino or hydrogen);
Z represents N--R8 (wherein R8 represents nitro, cyano, alkylsulfonyl, halogen substituted alkylsulfonyl, tosyl, alkylcarbonyl or halogen substituted alkylcarbonyl); or C(CN)R9, (wherein R9 is cyano or alkoxycarbonyl); and
A represents ethylene or C1 to C3 alkyl substituted ethylene;
excluding an organophosphorus compound of formula (I) in which R1 and R2 are C1 to C4 alkyl, X is NH, Z is cyanoimino or nitroimino, and A is ethylene or C1 to C3 alkyl substituted ethylene.
2. The organophosphorus compound according to claim 1 which is O-ethyl-S-n-propyl-(3-methyl-2-cyanoimino-1-imidazolidinyl) phosphonothiolate.
3. The organophosphorus compound according to claim 1 which is O-ethyl-S-n-propyl-(3-ethyl-2-cyanoimino-1-imidazolidinyl) phosphonothiolate.
4. The organophosphorus compound according to claim 1 which is O-ethyl-S-n-propyl-(2-dicyanomethylene-1-imidazolidinyl)phosphonothiolate.
5. The organophosphorus compound according to claim 1 which is O-ethyl-S-n-propyl-(2-methansulfonylimino-1-imidazolidinyl) phosphonothiolate.
6. The organophosphorus compound according to claim 1 which is O-ethyl-S-sec-butyl-(3-methyl-2-cyanoimino-1-imidazolidinyl) phosphonothiolate.
7. The organophosphorus compound according to claim 1 which is O-ethyl-S-n-propyl-(3-methyl-2-dicyanomethylene-1-imidazolidinyl) phosphonothiolate.
8. The organophosphorus compound according to claim 1 which is O-ethyl-S-sec-butyl-(3-methyl-2-dicyanomethylene-1-imidazolidinyl) phosphonothiolate.
9. The organophosphorus compound according to claim 1 which is O-ethyl-S-sec-butyl-(3-methoxymethyl-2-cyanoimino-1-imidazolidinyl) phosphonothiolate.
10. The organophosphorus compound according to claim 1 which is O-ethyl-S-n-propyl-[2-(2-cyano-2-ethoxycarbonylmethylene)-1-imidazolidinyl]-phosphonothiolate.
11. An insecticidal, acaricidal or nematocidal composition comprising a carrier and, as an active ingredient, an organophosphorus compound represented by formula (I) ##STR26## wherein R1 and R2 each represent C1 to C4 alkyl;
X represents NH or N--R4, wherein R4 represents C1 to C4 alkyl; C1 to C4 alkyl substituted with at least one group selected from the group consisting of alkoxy, alkylthio, cyano, alkoxyalkyloxy, alkylamino and halogen; alkenyl; halogen substituted alkenyl; alkynyl; halogen substituted alkynyl; phosphoric acid ester; cyano; a group of formula II: ##STR27## (wherein R5 represents alkyl, halogen substituted alkyl, alkylamino, or halogen substituted alkylamino); or --(R6) n --CO-- R7 (wherein n is 0 or 1; R6 represents methylene, alkyl substituted methylene, ethylene and alkyl substituted ethylene; and R7 represents alkyl, halogen substituted alkyl, alkoxy, halogen substituted alkoxy, alkylthio, alkylamino or hydrogen);
Z represents N--R8 (wherein R8 represents nitro, cyano, alkylsulfonyl, halogen substituted alkylsulfonyl, tosyl, alkylcarbonyl or halogen substituted alkylcarbonyl); or C(CN)R9, (wherein R9 is cyano or alkoxycarbonyl); and
A represents ethylene or C1 to C3 alkyl substituted ethylene;
excluding an organophosphorus compound of formula (I) in which R1 and R2 are C1 to C4 alkyl, X is NH, Z is cyanoimino or nitroimino, and A is ethylene or C1 to C3 alkyl substituted ethylene.
12. An insecticidal, acaricidal or nematocidal composition according to claim 11 wherein the active ingredient compound is O-ethyl-S-n-propyl-(3-methyl-2-cyanoimino-1-imidazolidinyl) phosphonothiolate.
13. An insecticidal, acaricidal or nematocidal composition according to claim 11 wherein the active ingredient compound is O-ethyl-S-n-propyl-(3-ethyl-2-cyanoimino-1-imidazolidinyl) phosphonothiolate.
14. An insecticidal, acaricidal or nematocidal composition according to claim 11 wherein the active ingredient compound is O-ethyl-S-n-propyl-(2-dicyanomethylene-1-imidazolidinyl) phosphonothiolate.
15. An insecticidal, acaricidal or nematocidal composition according to claim 11 wherein the active ingredient compound is O-ethyl-S-n-propyl-(2-methansulfonylimino-1-imidazolidinyl) phosphonothiolate.
16. An insecticidal, acaricidal or nematocidal composition according to claim 11 wherein the active ingredient compound is O-ethyl-S-sec-butyl-(3-methyl-2-cyanoimino-1-imidazolidinyl) phosphonothiolate.
17. An insecticidal, acaricidal or nematocidal composition according to claim 11 wherein the active ingredient compound is O-ethyl-S-n-propyl-(3-methyl-2-dicyanomethylene-1-imidazolidinyl) phosphonothiolate.
18. An insecticidal, acaricidal or nematocidal composition according to claim 11 wherein the active ingredient compound is O-ethyl-S-sec-butyl-(3-methyl-2-dicyanomethylene-1-imidazolidinyl) phosphonothiolate.
19. An insecticidal, acaricidal or nematocidal composition according to claim 11 wherein the active ingredient compound is O-ethyl-S-sec-butyl-(3-methoxymethyl-2-cyanoimino-1-imidazolidinyl) phosphonothiolate.
20. An insecticidal, acaricidal or nematocidal composition according to claim 11 wherein the active ingredient compound is O-ethyl-S-n-propyl-[2-(2-cyano-2-ethoxycarbonylmethylene)-1-imidazolidinyl]-phosphonothiolate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/104,909 US5405961A (en) | 1990-07-06 | 1993-08-12 | Organophosphorus compounds and insecticidal, acaricidal and nematocidal compositions containing same |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17882590 | 1990-07-06 | ||
| JP2-178825 | 1990-07-06 | ||
| JP3075327A JPH0739430B2 (en) | 1990-07-06 | 1991-04-08 | Organophosphorus compound, method for producing the same and insecticide, acaricide, nematicide containing the compound |
| JP3-75327 | 1991-04-08 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/104,909 Division US5405961A (en) | 1990-07-06 | 1993-08-12 | Organophosphorus compounds and insecticidal, acaricidal and nematocidal compositions containing same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US5280123A true US5280123A (en) | 1994-01-18 |
Family
ID=26416469
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/726,211 Expired - Lifetime US5280123A (en) | 1990-07-06 | 1991-07-05 | Organophosphorus compounds and its insecticides acaricides and nematocides containing same |
| US08/104,909 Expired - Lifetime US5405961A (en) | 1990-07-06 | 1993-08-12 | Organophosphorus compounds and insecticidal, acaricidal and nematocidal compositions containing same |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/104,909 Expired - Lifetime US5405961A (en) | 1990-07-06 | 1993-08-12 | Organophosphorus compounds and insecticidal, acaricidal and nematocidal compositions containing same |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US5280123A (en) |
| EP (1) | EP0464830B1 (en) |
| JP (1) | JPH0739430B2 (en) |
| KR (1) | KR940011223B1 (en) |
| CN (1) | CN1027670C (en) |
| DE (1) | DE69114925T2 (en) |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5405961A (en) * | 1990-07-06 | 1995-04-11 | Agro-Kanesho Co., Ltd. | Organophosphorus compounds and insecticidal, acaricidal and nematocidal compositions containing same |
| US5547965A (en) * | 1994-04-27 | 1996-08-20 | Bayer Aktiengesellschaft | Use of substituted amines for the treatment of brain function disorders |
| US6528079B2 (en) | 1996-06-04 | 2003-03-04 | Bayer Aktiengesellschaft | Shaped bodies which release agrochemical active substances |
| US6534529B2 (en) | 1995-12-27 | 2003-03-18 | Bayer Aktiengesellschaft | Synergistic insecticide mixtures |
| US20030134857A1 (en) * | 1998-06-23 | 2003-07-17 | Hermann Uhr | Synergistic insecticide mixtures |
| US6716874B1 (en) | 1999-03-24 | 2004-04-06 | Bayer Aktiengesellschaft | Synergistic insecticide mixtures |
| US20040127520A1 (en) * | 1998-05-26 | 2004-07-01 | Wolfram Andersch | Synergistic insecticidal mixtures |
| US20040235934A1 (en) * | 2000-05-19 | 2004-11-25 | Reiner Fischer | Active substance combinations having insecticidal and acaricdal properties |
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Cited By (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5405961A (en) * | 1990-07-06 | 1995-04-11 | Agro-Kanesho Co., Ltd. | Organophosphorus compounds and insecticidal, acaricidal and nematocidal compositions containing same |
| US5547965A (en) * | 1994-04-27 | 1996-08-20 | Bayer Aktiengesellschaft | Use of substituted amines for the treatment of brain function disorders |
| US6534529B2 (en) | 1995-12-27 | 2003-03-18 | Bayer Aktiengesellschaft | Synergistic insecticide mixtures |
| US7659228B2 (en) | 1995-12-27 | 2010-02-09 | Bayer Aktiengesellschaft | Synergistic insecticide mixtures |
| US6528079B2 (en) | 1996-06-04 | 2003-03-04 | Bayer Aktiengesellschaft | Shaped bodies which release agrochemical active substances |
| US6680065B2 (en) | 1996-06-04 | 2004-01-20 | Bayer Aktiengesellschaft | Shaped bodies which release agrochemical active substances |
| US20040127520A1 (en) * | 1998-05-26 | 2004-07-01 | Wolfram Andersch | Synergistic insecticidal mixtures |
| US7001903B2 (en) | 1998-05-26 | 2006-02-21 | Bayer Aktiengesellschaft | Synergistic insecticidal mixtures |
| US20030134857A1 (en) * | 1998-06-23 | 2003-07-17 | Hermann Uhr | Synergistic insecticide mixtures |
| US6828275B2 (en) | 1998-06-23 | 2004-12-07 | Bayer Aktiengesellschaft | Synergistic insecticide mixtures |
| US6894074B2 (en) | 1999-03-24 | 2005-05-17 | Bayer Aktiengesellschaft | Synergistic insecticidal mixtures |
| US6716874B1 (en) | 1999-03-24 | 2004-04-06 | Bayer Aktiengesellschaft | Synergistic insecticide mixtures |
| US8841294B2 (en) | 1999-10-07 | 2014-09-23 | Bayer Cropscience Ag | Active ingredient combinations having insecticidal and acaricidal properties |
| US6893651B1 (en) | 1999-10-07 | 2005-05-17 | Bayer Aktiengesellschaft | Active ingredient combinations having insecticidal and acaricidal properties |
| US20050187215A1 (en) * | 1999-10-07 | 2005-08-25 | Reiner Fischer | Active ingredient combinations having insecticidal and acaricidal properties |
| US20040235934A1 (en) * | 2000-05-19 | 2004-11-25 | Reiner Fischer | Active substance combinations having insecticidal and acaricdal properties |
| US7214701B2 (en) | 2000-05-19 | 2007-05-08 | Bayer Cropscience Ag | Active substance combinations having insecticidal and acaricdal properties |
| US6864276B2 (en) | 2000-05-19 | 2005-03-08 | Bayer Cropscience Ag | Active substance combinations having insecticidal and acaricidal properties |
| US20080033017A1 (en) * | 2000-11-30 | 2008-02-07 | Bayer Healthcare Llc | Compositions for enhanced acaricidal activity |
| US8232261B2 (en) | 2003-07-18 | 2012-07-31 | Bayer Cropscience Lp | Method of minimizing herbicidal injury |
| US8426339B2 (en) | 2003-07-18 | 2013-04-23 | Bayer Cropscience Lp | Method of minimizing herbicidal injury |
| US20050014646A1 (en) * | 2003-07-18 | 2005-01-20 | Schwarz Michael R. | Method of minimizing herbicidal injury |
| US20070157507A1 (en) * | 2004-08-25 | 2007-07-12 | Reid Byron L | Method of controlling termites |
| US9919979B2 (en) | 2005-01-21 | 2018-03-20 | Bayer Cropscience Lp | Fertilizer-compatible composition |
| US12425371B2 (en) * | 2022-09-16 | 2025-09-23 | Cisco Technology, Inc. | System and method for providing SCHC-based edge firewalling |
Also Published As
| Publication number | Publication date |
|---|---|
| DE69114925T2 (en) | 1996-05-30 |
| CN1027670C (en) | 1995-02-22 |
| EP0464830B1 (en) | 1995-11-29 |
| JPH04217991A (en) | 1992-08-07 |
| KR920002624A (en) | 1992-02-28 |
| EP0464830A1 (en) | 1992-01-08 |
| US5405961A (en) | 1995-04-11 |
| CN1058407A (en) | 1992-02-05 |
| DE69114925D1 (en) | 1996-01-11 |
| JPH0739430B2 (en) | 1995-05-01 |
| KR940011223B1 (en) | 1994-11-29 |
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